Chemical Reactivity of Pd-Au Bimetallic Nanoclusters Grown via Amorphous Solid Water as Buffer Layer

被引:18
作者
Gross, Elad [1 ]
Popov, Inna [2 ]
Asscher, Micha [1 ]
机构
[1] Hebrew Univ Jerusalem, Inst Chem, IL-91904 Jerusalem, Israel
[2] Hebrew Univ Jerusalem, Harvey M Krueger Family Ctr Nanosci & Nanotechnol, IL-91904 Jerusalem, Israel
基金
以色列科学基金会;
关键词
ACETYLENE HYDROGENATION; CATALYSIS; BENZENE; SURFACES; GOLD; NANOPARTICLES; ETHYLENE; CLUSTERS; AL2O3; FILMS;
D O I
10.1021/jp907614p
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Bimetallic Pd-Au nanoclusters were prepared on SiO2/Si(100) via amorphous solid water (ASW) as buffer layer. Selective growth pathways have led to segregated palladium and gold clusters or alloy bimetallic crystallites. Morphology and chemical composition were determined by AFM, SEM, and HR-TEM coupled to EDX analysis. Correlation between clusters morphology and composition to their chemical reactivity is reported for the first time. Temperature programmed reaction studies revealed that conversion of acetylene to ethylene and trimerization to benzene are significantly enhanced over crystalline alloy Pd-Au clusters when compared to clean Pd. A remarkable selectivity toward ethylene formation over benzene is unique to the alloy bimetallic clusters grown via ASW buffer layer on silica, presumably due to suppression of the trimerization pathway. The intrinsic, modified electronic properties of the bimetallic alloy clusters are believed to drive their enhanced chemical reactivity when compared with the pure Pd clusters.
引用
收藏
页码:18341 / 18346
页数:6
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